NP-MRD: Showing NP-Card for beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone (NP0054697)

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Record Information

Version

2.0

Created at

2022-04-28 00:58:17 UTC

Updated at

2022-04-28 00:58:17 UTC

NP-MRD ID

NP0054697

Secondary Accession Numbers

None

Natural Product Identification

Common Name

beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone

Description

NSC622370 belongs to the class of organic compounds known as linear 1,3-diarylpropanoids. These are organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together. Thus, NSC622370 is considered to be a flavonoid. beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone is found in Polygonum nepalense. Based on a literature review very few articles have been published on NSC622370.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282202582D          

 31 32  0  0  0  0            999 V2000
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 26  1  0  0  0  0
 26 27  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
  1 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 57 58  0  0  0  0  0  0  0  0999 V2000
    5.7122    0.6492   -3.0782 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9761    0.2428   -1.7512 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9149    0.2402   -0.8496 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497    0.6174   -1.2255 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6044    0.6024   -0.2906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3401    0.9855   -0.6980 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475    1.3788   -2.0357 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8831    0.2039    0.9979 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8456    0.1876    1.9930 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1510   -0.2240    3.1689 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4538    0.6093    1.7644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3704   -0.4645    1.1570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1669   -1.5618    0.9062 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7757   -0.2800    0.8469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4294    0.9230    1.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7749    1.0740    0.8059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4320    2.2636    1.0612 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7128    3.3242    1.6340 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5115    0.0554    0.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8223    0.2383   -0.0386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9218   -0.0061    0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8776   -1.1410   -0.0215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6243   -2.1668   -0.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7444   -2.3237   -1.9898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5203   -1.2920    0.2837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9009   -2.5043    0.0094 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2700   -2.7841   -1.2305 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1863   -0.1789    1.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2004   -0.1616    0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5053   -0.5384    0.7821 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7542   -0.9446    2.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8742    0.0798   -3.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6109    0.4602   -3.7173 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4810    1.7461   -3.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4388    0.9290   -2.2368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8634    2.2215   -2.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1026    1.7142   -2.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4363    0.5691   -2.7266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3515    1.5602    1.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0388    0.8712    2.7942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8452    1.7143    1.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1555    3.0047    2.5351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3534    4.1749    1.9265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9489    3.7454    0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1952    0.8226    1.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6411   -0.8630    1.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8171   -0.3634    0.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2177   -1.5172   -2.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8266   -2.2446   -2.2615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3899   -3.3106   -2.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0226   -3.3063   -1.8608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3844   -3.4214   -1.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9276   -1.8215   -1.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3793   -0.4900    2.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0582   -1.8176    2.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7968   -1.3071    2.2183 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4905   -0.1743    2.8607 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  2  0
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 14 25  2  0
 25 26  1  0
 26 27  1  0
 25 22  1  0
 22 23  1  0
 23 24  1  0
 22 19  2  0
 19 20  1  0
 20 21  1  0
 19 16  1  0
 16 17  1  0
 17 18  1  0
 16 15  2  0
 29  3  1  0
 15 14  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
 28 54  1  0
 31 55  1  0
 31 56  1  0
 31 57  1  0
 11 39  1  0
 11 40  1  0
 27 51  1  0
 27 52  1  0
 27 53  1  0
 24 48  1  0
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 24 50  1  0
 21 45  1  0
 21 46  1  0
 21 47  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 15 41  1  0
M  END


  Mrv1652304282202582D          

 31 32  0  0  0  0            999 V2000
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 26  1  0  0  0  0
 26 27  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
  1 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0054697

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C(C=C1OC)C(=O)CC(=O)C1=C(OC)C(OC)=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O9/c1-25-16-11-18(27-3)17(26-2)8-12(16)14(23)10-15(24)13-9-19(28-4)21(30-6)22(31-7)20(13)29-5/h8-9,11H,10H2,1-7H3

> <INCHI_KEY>
CHVACGOOXOYUAE-UHFFFAOYSA-N

> <FORMULA>
C22H26O9

> <MOLECULAR_WEIGHT>
434.441

> <EXACT_MASS>
434.157682417

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.297047709351574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(2,3,4,5-tetramethoxyphenyl)-3-(2,4,5-trimethoxyphenyl)propane-1,3-dione

> <ALOGPS_LOGP>
2.11

> <JCHEM_LOGP>
2.07366197

> <ALOGPS_LOGS>
-4.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.379053431112961

> <JCHEM_PKA_STRONGEST_BASIC>
-4.078357999222002

> <JCHEM_POLAR_SURFACE_AREA>
98.75000000000003

> <JCHEM_REFRACTIVITY>
111.86439999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.46e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(2,3,4,5-tetramethoxyphenyl)-3-(2,4,5-trimethoxyphenyl)propane-1,3-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.335 -12.320   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334 -16.170   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.000 -16.940   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.001 -14.630   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2    6   30                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    4   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16   26                                                  
CONECT   16   15   17   24                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   14                                                       
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   17   23                                                       
CONECT   23   22                                                            
CONECT   24   16   25                                                       
CONECT   25   24                                                            
CONECT   26   15   27                                                       
CONECT   27   26                                                            
CONECT   28    3   29                                                       
CONECT   29   28                                                            
CONECT   30    1   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₉

Average Mass

434.4410 Da

Monoisotopic Mass

434.15768 Da

IUPAC Name

1-(2,3,4,5-tetramethoxyphenyl)-3-(2,4,5-trimethoxyphenyl)propane-1,3-dione

Traditional Name

1-(2,3,4,5-tetramethoxyphenyl)-3-(2,4,5-trimethoxyphenyl)propane-1,3-dione

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(C=C1OC)C(=O)CC(=O)C1=C(OC)C(OC)=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C22H26O9/c1-25-16-11-18(27-3)17(26-2)8-12(16)14(23)10-15(24)13-9-19(28-4)21(30-6)22(31-7)20(13)29-5/h8-9,11H,10H2,1-7H3

InChI Key

CHVACGOOXOYUAE-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Polygonum nepalense	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear 1,3-diarylpropanoids. These are organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Not Available

Direct Parent

Linear 1,3-diarylpropanoids

Alternative Parents

Substituents

Linear 1,3-diarylpropanoid
Alkyl-phenylketone
Butyrophenone
Phenylketone
Anisole
Benzoyl
Methoxybenzene
Phenol ether
Aryl alkyl ketone
Aryl ketone
Phenoxy compound
Alkyl aryl ether
1,3-diketone
Monocyclic benzene moiety
1,3-dicarbonyl compound
Benzenoid
Ketone
Ether
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120400 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.11	ALOGPS
logP	2.07	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	8.38	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	98.75 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	111.86 m³·mol⁻¹	ChemAxon
Polarizability	44.3 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00006998

Chemspider ID

319876

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

360323

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone (NP0054697)

MOL for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

3D MOL for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

3D SDF for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

3D-SDF for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

PDB for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

3D PDB for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

SMILES for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

INCHI for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

Structure for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)

3D Structure for NP0054697 (beta-Hydroxy-2,3,4,5,2',4',5'-heptamethoxychalcone)